US2010279404A1PendingUtilityA1
Method of nuclear reprogramming
Est. expiryMay 2, 2028(~1.8 yrs left)· nominal 20-yr term from priority
C12N 2506/13C12N 2501/603C12N 2501/602C12N 15/79C12N 2501/606C12N 2506/1361C12N 2506/1307C12N 2510/00C12N 5/0606C12N 5/0696C12N 2501/604C12N 2506/02C12N 2501/605C12N 2501/608H01J 37/241H01J 37/32073H01J 2237/038H01J 2237/06375
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Claims
Abstract
This invention provides a method of producing an induced pluripotent stem cell comprising the step of introducing at least one kind of non-viral expression vector (more preferably a plasmid vector) incorporating at least one gene that encodes a reprogramming factor into a somatic cell. An induced pluripotent stem cell wherein no exogenous genes induced is integrated into the cellular genome is also provided.
Claims
exact text as granted — not AI-modified1 . A method of producing an induced pluripotent stem cell, comprising the step of introducing at least one kind of non-viral expression vector incorporating at least one gene that encodes a reprogramming factor into a somatic cell.
2 . The method of claim 1 , wherein the vector is a non-viral expression vector autonomously replicable outside a chromosome.
3 . The method of claim 1 , wherein the vector is a plasmid vector.
4 . (canceled)
5 . The method of claim 1 , wherein the gene that encodes a reprogramming factor is one or more kind of genes selected from the group consisting of an Oct family gene, a Klf family gene, a Sox family gene, a Myc family gene, a Lin family gene, and the Nanog gene.
6 . The method of claim 1 , wherein the gene that encodes a reprogramming factor is one of the following combinations:
(a) a combination of two kinds of genes consisting of an Oct family gene and a Sox family gene; (b) a combination of three kinds of genes consisting of an Oct family gene, a Klf family gene, and a Sox family gene; (c) a combination of four kinds of genes consisting of an Oct family gene, a Klf family gene, a Sox family gene, and a Myc family gene; (d) a combination of four kinds of genes consisting of an Oct family gene, a Sox family gene, a Lin family gene, and the Nanog gene; and (e) a combination of six kinds of genes consisting of an Oct family gene, a Sox family gene, a Klf family gene, a Myc family gene, a Lin family gene, and the Nanog gene, or any one of these combinations further comprising the TERT gene and/or the SV40 Large T antigen gene.
7 . The method of claim 1 , wherein the gene that encodes a reprogramming factor is one of the following combinations:
(a) a combination of two kinds of genes consisting of Oct3/4 and Sox2; (b) a combination of three kinds of genes consisting of Oct3/4, Klf4, and Sox2; (c) a combination of four kinds of genes consisting of Oct3/4, Klf4, Sox2, and c-Myc; (d) a combination of four kinds of genes consisting of Oct3/4, Sox2, Lin28, and Nanog; and (e) a combination of six kinds of genes consisting of Oct3/4, Sox2, Klf4, c-Myc, Lin28, and Nanog, or any one of these combinations further comprising the TERT gene and/or the SV40 Large T antigen gene.
8 . The method of claim 1 , wherein the number of kinds of non-viral expression vectors introduced into the somatic cell is 1, 2, 3, or 4.
9 . The method of claim 8 , wherein the gene that encodes a reprogramming factor is a combination of three kinds of genes consisting of an Oct family gene, a Klf family gene, and a Sox family gene, or a combination of four kinds of genes consisting of an Oct family gene, a Klf family gene, a Sox family gene, and a Myc family gene, wherein the Oct family gene, the Klf family gene, and the Sox family gene are incorporated in one kind of non-viral expression vector.
10 . The method of claim 9 , wherein the Oct family gene, the Klf family gene, and the Sox family gene are incorporated in one kind of non-viral expression vector in this order in the orientation from the 5′ to 3′ end.
11 . The method of claim 9 , wherein the Oct family gene, the Klf family gene, and the Sox family gene are incorporated in one kind of non-viral expression vector with an intervening sequence enabling polycistronic expression.
12 . The method of claim 9 , wherein the Oct family gene is Oct3/4, the Klf family gene is Klf4, the Sox family gene is Sox2, and the Myc family gene is c-Myc.
13 . The method of claim 9 , wherein a first non-viral expression vector and a second non-viral expression vector are concurrently introduced into a somatic cell.
14 . The method of claim 13 , wherein said introduction is repeatedly performed twice or more.
15 . The method of claim 1 , wherein the somatic cell is a somatic cell of a mammal, including a human.
16 . An induced pluripotent stem cell that can be obtained by the method of claim 1 .
17 . The induced pluripotent stem cell of claim 16 , wherein whole or part of the at least one non-viral expression vector introduced is substantially not integrated in the chromosome.
18 . A non-viral expression vector incorporating a gene that encodes at least one reprogramming factor.
19 . The vector of claim 18 , wherein the vector is a plasmid vector.
20 . The vector of claim 18 , wherein an Oct family gene, a Klf family gene, and a Sox family gene are incorporated.
21 . The vector of claim 20 , wherein the Oct family gene, the Klf family gene, and the Sox family gene are incorporated in this order in the orientation from the 5′ to 3′ end.
22 . The vector of claim 21 , wherein the Oct family gene, the Klf family gene, and the Sox family gene are incorporated via a sequence enabling polycistronic expression.
23 . The vector of claim 20 , wherein the Oct family gene is Oct3/4, the Klf family gene is Klf4, and the Sox family gene is Sox2.
24 . An induced pluripotent stem cell wherein one or more transgenes encoding reprogramming factor are integrated into the cellular genome in the form of plasmid.
25 . An induced pluripotent stem cell wherein no exogenous genes introduced is integrated into the cellular genome.
26 . The vector of claim 18 , harboring genes encoding two or more kinds of reprogramming factors, wherein the genes are incorporated via 2A sequence derived from foot-and-mouth disease virus.Cited by (0)
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